20
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T73586 | Anticonvulsant agent 2 | Others | |
Anticonvulsant agent 2 is a potent orally active anticonvulsant that has shown antiepileptic activity in a model of drug-resistant epilepsy. | |||
T10027 | Anticonvulsant agent 1 | 4-(2,2-Difluoroethenyl)-α-ethyl-2-oxo-1-pyrrolidineacetamide | Others |
Anticonvulsant agent 1 is an anticonvulsant compound. | |||
T3563 | Lvguidingan | Others | |
Lvguidingan is an Anticonvulsant agent. | |||
T8588 | Buramate | Antibacterial | |
Buramate is an antipsychotic and anticonvulsant. | |||
T5563 | Cyclohexanecarboxylic Acid | Others , Endogenous Metabolite | |
Cyclohexanecarboxylic acid is a flavouring ingredien | |||
T15545 | ICA-27243 | Potassium Channel | |
ICA-27243 is less effective at activating KCNQ4 and KCNQ3/Q5. ICA-27243 is a potent and orally active KCNQ2/Q3 potassium channel opener (EC50: 0.38 μM). ICA-27243 also has antiepileptic and anticonvulsant effects. | |||
T0413 | Cinromide | trans-3-Bromo-N-ethylcinnamamide | Others |
Cinromide (trans-3-Bromo-N-ethylcinnamamide) is used as a novel anticonvulsant agent. | |||
T6259 | Dizocilpine | MK-801 | NMDAR , iGluR |
MK-801 (Dizocilpine (MK-801)) is a potent N-methyl-D-aspartate (NMDA) receptor antagonist with Ki of 30.5 nM. | |||
T0600 | 10,11-Dihydrocarbamazepine | Dihydrocarbamazepine | Others |
10,11-Dihydrocarbamazepine (Dihydrocarbamazepine) is used as pharmaceutical intermediates. | |||
T22675 | Co 102862 | V 102862 | Others , Sodium Channel |
Co 102862 is a voltage-gated sodium channel blocker. Co 102862 can be used for anticonvulsant studies. | |||
T7780 | Blarcamesine | AE-37,AVex-73 | AChR |
Blarcamesine (AVex-73) is a muscarinic M1 agonist potentially for the treatment of Alzheimer's disease. | |||
T8014 | Epoxylinalool | 2-(2-Hydroxy-2-Propyl)-5-Methyl-5-Vinyltetrahydrofuran | Others |
Epoxylinalool (2-(2-Hydroxy-2-Propyl)-5-Methyl-5-Vinyltetrahydrofuran) is a naturally occurring monoterpene alcohol widely used in the production of perfumes and flavors. | |||
T0440 | Oxcarbazepine | GP 47680 | Apoptosis , Sodium Channel |
Oxcarbazepine (GP 47680) is an Anti-epileptic Agent. The physiologic effect of oxcarbazepine is by means of Decreased Central Nervous System Disorganized Electrical Activity. | |||
T0283 | Trimethadione | 3,5,5,-Trimethyloxazolidine-2,4-dione | Calcium Channel |
Trimethadione (3,5,5,-Trimethyloxazolidine-2,4-dione) is a dione-type anticonvulsant with antiepileptic activity. | |||
TP2036L | DPDPE TFA (88373-73-3 free base) | DPDPE TFA | Opioid Receptor |
DPDPE TFA is selective δ-opioid receptor agonist peptide. Inhibits electrically stimulated contraction of mouse vas deferens in vitro (EC50 = 5.2 nM), and is antinociceptive in vivo. | |||
T3248 | Alpha-Boswellic acid | α-Boswellic acid | Others |
alpha-Boswellic acid (α-Boswellic acid) is a pentacyclic triterpenoid natural product extracted from frankincense and has anticonvulsant and anticancer effects. In animals, it prevents and reduces Alzheimer's disease mar... | |||
T4118 | SB 271046 hydrochloride | SB 271046A | 5-HT Receptor |
SB 271046 hydrochloride (SB 271046A) is selective, orally active 5-HT6 antagonist (pKi values are 9.02-8.92, 6.35, 6.55, 6.27 at 5-HT6, 5-HT1A, 5-HT1D and D3, and 6.05, 5.95, 5.76, 5.73, 5.62, 5.55, 5.41, 5.39, 5.27 and ... | |||
T0992 | Carbenoxolone disodium | Biogastrone,Duogastrone,Bioral | Gap Junction Protein |
Carbenoxolone disodium (Duogastrone) salt is an agent derived from licorice root. It is used for the treatment of digestive tract ulcers, especially in the stomach. Antidiuretic side effects are frequent, but otherwise, ... | |||
TP2036 | DPDPE | Opioid Receptor | |
DPDPE is selective δ-opioid receptor agonist peptide. Inhibits electrically stimulated contraction of mouse vas deferens in vitro (EC50 = 5.2 nM), and is antinociceptive in vivo. | |||
T14983 | Clomethiazole | Distraneurin,Chlormethiazole,5-(2-CHLOROETHYL)-4-METHYLTHIAZOLE | P450 , GABA Receptor |
Clomethiazole (Distraneurin) is an orally active GABAA agonist and it is an anticonvulsant agent. It also has the potential for treating convulsive status epilepticus. Chlormethiazole inhibits cytochrome P450 isoforms: C... |